Canonical Allele Identifier: CA1162036848

Linked Data

dbSNP Id: rs1640234617

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34794141T>A , CM000663.2:g.34794141T>A GRCh38
NC_000001.10:g.35259742T>A , CM000663.1:g.35259742T>A GRCh37
NC_000001.9:g.35032329T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342280.5:c.-17-56T>A (GJA4) MANE Select ENSP00000343676.4:n.-17-56T>A
ENST00000342280.4:c.-17-56T>A (GJA4) ENSP00000343676.4:n.-17-56T>A
ENST00000426886.1:c.207+61630A>T (SMIM12) ENSP00000429902.1:n.207+61630A>T
ENST00000450137.1:c.-73T>A (GJA4) ENSP00000409186.1:n.-73T>A
NM_002060.2:c.-17-56T>A (GJA4) NP_002051.2:n.-17-56T>A
XM_005270750.1:c.-73T>A (GJA4) XP_005270807.1:n.-73T>A
XR_947179.1:n.1001+4230A>T
XM_005270750.2:c.-73T>A (GJA4) XP_005270807.1:n.-73T>A
XM_017001043.2:c.-17-56T>A (GJA4) XP_016856532.1:n.-17-56T>A
XR_001737967.1:n.1023+4230A>T
NM_002060.3:c.-17-56T>A (GJA4) MANE Select NP_002051.2:n.-17-56T>A